Associated Disease N. genes N. variants N. of shared genes JI g p-value g N. of shared variants JI v p-value v
Estren-Dameshek Variant of Fanconi Anemia
1 0 1 1.00 0 0
Growth retardation, pre- and postnatal
3 0 1 0.33 0 0
FANCONI ANEMIA, COMPLEMENTATION GROUP N
4 0 1 0.25 0 0
CUI: C4025639
Disease: Prolonged G2 phase of cell cycle
Prolonged G2 phase of cell cycle
4 0 1 0.25 0 0
Deficient excision of UV-induced pyrimidine dimers in DNA
4 0 1 0.25 0 0
Complete duplication of thumb phalanx
8 0 1 0.12 0 0
Chromosomal breakage induced by crosslinking agents
8 0 1 0.12 0 0
CUI: C4025811
Disease: Anemic pallor
Anemic pallor
8 0 1 0.12 0 0
CUI: C3826743
Disease: Anemia in children
Anemia in children
9 0 1 0.11 0 0
CUI: C0858867
Disease: Reticulocytopenia
Reticulocytopenia
17 0 1 5.9E-02 0 0
CUI: C1858565
Disease: Duplicated collecting system
Duplicated collecting system
19 0 1 5.3E-02 0 0
CUI: C0037231
Disease: Sjogren-Larsson Syndrome
Sjogren-Larsson Syndrome
20 0 1 5.0E-02 0 0
CUI: C0241391
Disease: Thumb absent
Thumb absent
21 0 1 4.8E-02 0 0
CUI: C3278811
Disease: Thumb aplasia
Thumb aplasia
22 0 1 4.5E-02 0 0
CUI: C4022016
Disease: Abnormality of the preputium
Abnormality of the preputium
22 0 1 4.5E-02 0 0
CUI: C4023917
Disease: Aplasia/Hypoplasia of the uvula
Aplasia/Hypoplasia of the uvula
22 0 1 4.5E-02 0 0
CUI: C4025071
Disease: Aplasia/Hypoplasia of fingers
Aplasia/Hypoplasia of fingers
22 0 1 4.5E-02 0 0
CUI: C2242817
Disease: Homocysteine measurement
Homocysteine measurement
23 0 1 4.3E-02 0 0
CUI: C0037290
Disease: Skin Pigmentation
Skin Pigmentation
24 0 1 4.2E-02 0 0
Pyridoxine-responsive sideroblastic anemia
24 0 1 4.2E-02 0 0
CUI: C0342526
Disease: Absent testes
Absent testes
24 0 1 4.2E-02 0 0
CUI: C1405984
Disease: Absent radius
Absent radius
24 0 1 4.2E-02 0 0
CUI: C0432470
Disease: 46, XY female
46, XY female
25 0 1 4.0E-02 0 0
CUI: C0015624
Disease: Fanconi Syndrome
Fanconi Syndrome
26 0 1 3.8E-02 0 0
CUI: C0025209
Disease: Melanosis
Melanosis
26 0 1 3.8E-02 0 0